Report ID: SQMIG35H2239
Report ID:
SQMIG35H2239 |
Region:
Global |
Published Date: March, 2024
Pages:
219
|
Tables:
96 |
Figures:
76
In June 2022, CNS Pharmaceuticals, Inc. received approval from the U.S. Food and Drug Administration (FDA) for its ongoing potentially pivotal global study evaluating the efficacy and safety of Berubicin compared with Lomustine (Gleostine) administered after first-line therapy for the treatment of recurrent glioblastoma multiforme (GBM), one of the most aggressive types of brain cancer.
In January 2022, Otsuka Pharmaceutical Co., Ltd. (Otsuka); its subsidiary Otsuka America Pharmaceutical, Inc.; and Lundbeck, Inc., a U.S. subsidiary of H. Lundbeck A/S in Denmark, announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental new drug application (sNDA) of REXULTI (brexpiprazole) for the treatment of schizophrenia in pediatric patients 13 to 17 years of age.
In April 2021, Biogen acquired the approval of the National Medical Products Administration for its product TECFIDERA for the treatment of relapsing multiple sclerosis in China.
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Report ID: SQMIG35H2239